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World Journal of Medical Genetics|March 28, 2017
Mutation in TNXB gene causes moderate to severe Ehlers-Danlos syndromeCarolyn S Kaufman, Merlin G ButlerJournal of Pediatric Genetics|September 13, 2016
A Case of the 7p22.2 Microduplication: Refinement of the Critical Chromosome Region for 7p22 Duplication SyndromeDevin M Cox, Merlin G ButlerMedical Anthropology Quarterly|October 4, 2016
Characterization of Obesity in the Prader-Labhart-Willi Syndrome: Fatness PatterningF John Meaney, Merlin G ButlerGenes|February 26, 2025
Systematic Review: Fragile X Syndrome Across the Lifespan with a Focus on Genetics, Neurodevelopmental, Behavioral and Psychiatric AssociationsAnn C Genovese, Merlin G ButlerAmerican Journal of Medical Genetics. Part A|October 3, 2022
Prader-Willi syndrome, deletion subtypes, and magnesium: Potential impact on clinical findingsMerlin G Butler, Neil Cowen, Anish BhatnagarFrontiers in Genetics|December 17, 2020
Pharmacodynamic Gene Testing in Prader-Willi SyndromeJanice Forster, Jessica Duis, Merlin G ButlerInternational Journal of Molecular Sciences|October 14, 2022
Genetics of Obesity in Humans: A Clinical ReviewRanim Mahmoud, Virginia Kimonis, Merlin G ButlerGenes|September 27, 2025
RNA Polymerase I Dysfunction Underlying Craniofacial Syndromes: Integrated Genetic Analysis Reveals Parallels to 22q11.2 Deletion SyndromeSpencer Silvey, Scott Lovell, Merlin G ButlerInternational Journal of Molecular Sciences|February 11, 2023
Clinical Trials in Prader-Willi Syndrome: A ReviewRanim Mahmoud, Virginia Kimonis, Merlin G ButlerHearing Research|August 19, 2005
Biotinidase reveals the morphogenetic sequence in cochlea and cochlear nucleus of miceCraig L Brumwell, Waheeda A Hossain, D Kent Morest, et al.Pageof 24